A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867473



Internal ID22642408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71945339..71946650hg38UCSC Ensembl
chr10:73705097..73706408hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381312
hg191312
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449945
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867473
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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